Viewing Study NCT05467592


Ignite Creation Date: 2025-12-24 @ 3:58 PM
Ignite Modification Date: 2026-02-26 @ 7:25 PM
Study NCT ID: NCT05467592
Status: COMPLETED
Last Update Posted: 2025-05-20
First Post: 2022-05-16
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Central Sensitization in Patients Seeking Outpatient Physical Therapy Services
Sponsor: University of Kansas Medical Center
Organization:

Study Overview

Official Title: Central Sensitization in Patients Seeking Outpatient Physical Therapy Services
Status: COMPLETED
Status Verified Date: 2025-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is an observational study to examine presence of CS in patients with knee osteoarthritis (OA), chronic LBP (CLBP), and chronic neck pain (CNP) seeking outpatient physical therapy (PT) services. The study will also examine if outcomes differ between patients with CS and patients without CS symptoms with standard PT interventions.
Detailed Description: Central Sensitization (CS), defined as augmented pain processing, is common in subgroup of nearly all chronic pain conditions, including fibromyalgia, CLBP, OA, and chronic tension headache. However, current studies of CS are primarily limited to research settings, lacking the knowledge about prevalence of CS and rehabilitation outcomes in usual clinical care.

Practicing clinicians do not routinely assess for CS symptoms. Without proper screening for CS, and lack of knowledge of varying levels of nervous system involvement contributing to pain, clinicians are unable to fully identify the depth of the mechanisms and therefore unable to fully determine the best treatment strategies. This observational study addresses this gap in knowledge by screening patients for CS symptoms.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: